Site Start-Up Specialist (UK) - IQVIA Biotech (R1112500) in Stevenage, UK at IQVIA™

Date Posted: 1/30/2020

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Stevenage, UK
  • Experience:
    Not Specified
  • Date Posted:
    1/30/2020
  • Job ID:
    R1112500

Job Description

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

IQVIA Biotech has an exciting position within its Start-up team.

We're looking for a lively, enthusiastic and independent professionals who are willing to work from home with an international EU team.

IQVIA Biotech specialises in working with smaller biotech and emerging biopharma clients and as such we have a vibrant, fast-paced work environment. You’ll be working with a lot of the new innovative and upcoming research groups across a variety of therapy areas.
 

•   Supports the Site Feasibility Lead or representative to provide updates during weekly client teleconferences and internal team meetings, as required.
•    Liaise with Clinical Monitoring, Site Start Up Lead, Regulatory Affairs, other interdepartmental team members, and sponsor to enable a rapid clinical trial start-up.
•    May participate in the drafting of the feasibility questionnaire for a study.
•    Will assist in the dissemination of Confidential Disclosure Agreements (CDAs) and feasibility questionnaires to sites and follow up with sites accordingly to ascertain interest and to meet study timelines.
•    Participate in the review and negotiation of the CDAs according to country specific requirements.
•    Adheres to study timelines, documents/escalates study challenges, and communicates updates to Project Manager and SSU Lead/Management.
•    Maintains quality and regulatory compliance among investigational sites during Site Feasibility.
•    Maintains up to date and accurate tracking on the Site Feasibility status for each site in applicable system(s) for the study.  
•    Liaise with team members to understand budgets for the studies they are working on and are accountable for maintaining project activities within documented scope and budget.
•    Identifies out of scope activities to Site Feasibility Management, Project Manager and team and assures that such activities do not begin until the appropriate authorization is provided.
•    Responsible for transitioning sites from Site Feasibility to SSU representative.
•    Provides updates to Lead/Manager on a regular basis and communicates any out of scope activities.
•    Participates in financial and/or resource forecasting, as applicable. 
•    Performs other duties as required.

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.



Job ID: R1112500